Clinical Research Coordinator 1 (A)

University of Miami; United States; Sur place; USD 50 000 - 65 000; Plein temps

Avantages offerts par ce poste

Medical benefits

Tuition remission

Résumé du poste

University of Miami's Psychiatry department is seeking a full-time Clinical Research Coordinator 1 on the UHealth campus. The role supports entry-level clinical research with data management and protocol implementation, handling simple studies and timelines.

The position requires a Bachelor's degree and at least 1 year of relevant experience, with flexibility to work evenings or weekends as needed. You will coordinate data collection, enrollment procedures, IRB compliance, and basic data

Qualifications

• Bachelor’s degree in a relevant field.
• Minimum 1 year of relevant experience.
• Skill in completing assignments accurately and with attention to detail.
• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
• Ability to process and handle confidential information with discretion.
• Ability to work evenings, nights, and weekends as necessary.

Responsabilités

• Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
• Maintains enrollment procedures according to the protocol.
• Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
• Performs moderate to complex research tests/experiments and adapts procedures for quality improvement under supervision.
• Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
• Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.
• Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
• Proficiency in building, modifying and maintaining REDcap database for the study.

Connaissances

Attention to detail

Discretion with confidential data

Time management

Independent & collaborative work

Formation

Bachelor’s degree in relevant field

Outils

REDCap database

Description du poste

The department of Psychiatry has an exciting opportunity for a full-time Clinical Research Coordinator 1 to work on the UHealth campus.

The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols.

This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.

CORE JOB FUNCTIONS

• Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
• Maintains enrollment procedures according to the protocol.
• Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
• Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.

DEPARTMENT SPECIFIC FUNCTIONS

• Engage in basic project coordination which include developing project goals, submitting IRB documents and all compliance documents.
• Assist with development of scientific scholarship products such as manuscripts, PowerPoint, etc.
• Assist with basic data analysis.
• Engages with community stakeholders and coordinates recruitment activities.
• Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
• Maintains enrollment procedures according to the protocol.
• Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, administering surveys and project evaluation.
• Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.
• Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.
• Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
• Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
• Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.
• Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
• Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
• Proficiency in building, modifying and maintaining REDcap database for the study.
• Adheres to cultural competency guidelines; implements strategies to meet study participants' needs for language translation, health literacy, etc.
• Assists in administrative tasks and documenting core competencies.
• Coordinates routine activities of clinical studies including data maintenance, grant expenditure adherence, project evaluation, meeting scheduling, and research subject interfacing.
• Tracks medical reports and reviews regulatory documents to generate reports.
• Serves as project liaison to other departments, outside organizations, government agencies, and product representatives.
• Recruits patients into the study and reviews on a weekly basis the percentage recruited.
• Reviews data collected and inserts into the study dataset.
• Compares the data collected to the monitored phone calls for data quality assurance.
• Evaluates and monitors timelines for studies and for each subject participant to comply with applicable protocols.
• Prepares materials for the brochures and retaining letters and mails to appropriate members according to their time in the study.
• Administers informed consent forms for patients on drug studies.
• Maintains pool of study candidates and ensures their availability.

CORE QUALIFICATIONS

• Bachelor’s degree in relevant field
• Minimum 1 year of relevant experience
• Skill in completing assignments accurately and with attention to detail.
• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
• Ability to process and handle confidential information with discretion.
• Ability to work evenings, nights, and weekends as necessary.
• Commitment to the University’s core values.
• Ability to work independently and/or in a collaborative environment.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Job Status: Full time Employee Type: Staff

The mission of the University of Miami is to transform lives through education, research, innovation, and service. A vibrant and diverse academic and healthcare community, the University of Miami and the University of Miami Health System ("UHealth") have rapidly progressed to become one of the nation’s top research universities and academic medical centers in the nation. The University comprises 12 schools and colleges serving undergraduate and graduate students in more than 350 majors and programs. Visit welcome.miami.edu/about-um to learn more about our points of pride. The University ranks No. 55 on U.S. News & World Report’s 2022 Best Colleges list and ranked No. 49 in the 2022 Wall Street Journal/Times Higher Education College Rankings. Bascom Palmer Eye Institute is ranked the #1 eye hospital in the USA and offers some of the nation's premiere eye doctors to treat every eye condition for adults. Sylvester Comprehensive Cancer, part of the Miller School of Medicine, received the prestigious National Cancer Institute designation in 2019. The University of Miami and UHealth have also ranked among the Forbes Best Employers and Best Employers for Women on several occasions, most recently in 2022. With more than 17,000 faculty and staff, the University strives for excellence, and is driven by a powerful mission to transform and impact the lives of its students, patients, members of the community, and people across the globe.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.